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HRID 12886作成日:2026年10月26日

2-Propenoic acid, 2-cyano-3-ethoxy-, ethyl ester → ethyl 5-amino-1-cyclopentyl-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/12886

反応式

関与物質

役割名称HCID仕込み量
反応物2-Propenoic acid, 2-cyano-3-ethoxy-, ethyl esterHCID 78943—
反応物Cyclopentylhydrazine hydrochlorideHCID 212349—
反応物Sodium AcetateHCID 517045—
溶媒EthanolHCID 702—
生成物ethyl 5-amino-1-cyclopentyl-1H-pyrazole-4-carboxylateHCID 1250812679.3%

反応条件

温度70 °C

反応手順

Cyclopentyl-hydrazine hydrochloride (1.000 g; 7.32 mmol), ethyl (ethoxymethylene)-cyanoacetate (1.026 g, 6.61 mmol) and anhydrous sodium acetate (0.644 g, 7.85 mmol) were combined in ethanol (10 mL) and heated at 70° C. for 20 hours. After cooling to room temperature, ethanol was removed in vacuo and the residue was partitioned between methylene chloride and water. The organic phase was washed sequentially with water and brine. Each aqueous phase was back extracted with a single portion of methylene chloride. The two organic phases were combined, dried over sodium sulfate and concentrated. Purification by flash chromatography, eluting with 10-40% EtOAc/hexanes yielded 5-amino-1-cyclopentyl-1H-pyrazole-4-carboxylic acid ethyl ester (1.170 g, 73%). Mass spectrum: m/z: 224.1 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728029B2
出典データセットuspto-grants-2010_06
ORD IDord-660058880d6144ccbdfae5625f97875b
出典メモuspto-grants-2010_06